Variant report

Variant	nsv593572
Chromosome Location	chr4:7427899-7437364
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:7431462-7431555	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr4:7436571-7436572	HepG2	liver:	n/a	n/a
3	CEBPB	chr4:7433508-7433674	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr4:7433501-7433762	MCF-7	breast:	n/a	n/a
5	CEBPB	chr4:7433460-7433830	MCF-7	breast:	n/a	n/a
6	CHD2	chr4:7436619-7436861	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr4:7433640-7433790	HMEC	breast:	n/a	n/a
8	CTCF	chr4:7436683-7436741	LNCaP	prostate:	n/a	chr4:7436701-7436719
9	CTCF	chr4:7435308-7435402	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr4:7432277-7432412	NHEK	skin:	n/a	n/a
11	CTCF	chr4:7435240-7435390	AG04449	skin:	n/a	n/a
12	CTCF	chr4:7432400-7432550	HRE	kidney:	n/a	n/a
13	CTCF	chr4:7432260-7432410	HMEC	breast:	n/a	n/a
14	CTCF	chr4:7432240-7432390	NHEK	skin:	n/a	n/a
15	CTCF	chr4:7435260-7435410	HBMEC	blood vessel:	n/a	n/a
16	CTCF	chr4:7432316-7432365	MCF-7	breast:	n/a	n/a
17	E2F4	chr4:7436626-7436856	MCF10A-Er-Src	breast:	n/a	n/a
18	EGR1	chr4:7433472-7433889	MCF-7	breast:	n/a	n/a
19	FOS	chr4:7436572-7436866	MCF10A-Er-Src	breast:	n/a	chr4:7436730-7436738 chr4:7436729-7436740
20	FOS	chr4:7436573-7436878	MCF10A-Er-Src	breast:	n/a	chr4:7436730-7436738 chr4:7436729-7436740
21	FOS	chr4:7433600-7433663	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr4:7436578-7436862	MCF10A-Er-Src	breast:	n/a	chr4:7436730-7436738 chr4:7436729-7436740
23	FOS	chr4:7436597-7436862	MCF10A-Er-Src	breast:	n/a	chr4:7436730-7436738 chr4:7436729-7436740
24	FOSL2	chr4:7436508-7436891	HepG2	liver:	n/a	chr4:7436730-7436738 chr4:7436729-7436740
25	FOXA2	chr4:7433379-7433710	A549	lung:	n/a	n/a
26	FOXA2	chr4:7433240-7433711	A549	lung:	n/a	n/a
27	FOXA2	chr4:7437238-7437500	HepG2	liver:	n/a	n/a
28	JUND	chr4:7436635-7436850	H1-hESC	embryonic stem cell:	n/a	chr4:7436730-7436738 chr4:7436728-7436739 chr4:7436729-7436740
29	JUND	chr4:7436533-7436871	A549	lung:	n/a	chr4:7436730-7436738 chr4:7436728-7436739 chr4:7436729-7436740
30	JUND	chr4:7436652-7436849	K562	blood:	n/a	chr4:7436730-7436738 chr4:7436728-7436739 chr4:7436729-7436740
31	JUND	chr4:7436677-7436865	HepG2	liver:	n/a	chr4:7436730-7436738 chr4:7436728-7436739 chr4:7436729-7436740
32	JUND	chr4:7436609-7436834	HepG2	liver:	n/a	chr4:7436730-7436738 chr4:7436728-7436739 chr4:7436729-7436740
33	KAP1	chr4:7436633-7436966	U2OS	brain:	n/a	n/a
34	MAZ	chr4:7437184-7437199	HepG2	liver:	n/a	n/a
35	MAZ	chr4:7436590-7436813	Hela-S3	cervix:	n/a	n/a
36	MAZ	chr4:7436715-7436887	HepG2	liver:	n/a	n/a
37	MYC	chr4:7433514-7433754	MCF10A-Er-Src	breast:	n/a	n/a
38	MYC	chr4:7432257-7432363	MCF-7	breast:	n/a	n/a
39	NR3C1	chr4:7431693-7431949	A549	lung:	n/a	chr4:7431900-7431913
40	NR3C1	chr4:7431606-7432058	A549	lung:	n/a	chr4:7431900-7431913 chr4:7432012-7432021
41	NR3C1	chr4:7432094-7432335	A549	lung:	n/a	n/a
42	POLR2A	chr4:7432200-7432220	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr4:7435661-7435688	MCF-7	breast:	n/a	n/a
44	POLR2A	chr4:7436568-7436901	HCT-116	colon:	n/a	n/a
45	RAD21	chr4:7436604-7436836	H1-hESC	embryonic stem cell:	n/a	chr4:7436699-7436718 chr4:7436703-7436717
46	RAD21	chr4:7436693-7436806	Hela-S3	cervix:	n/a	chr4:7436699-7436718 chr4:7436703-7436717
47	RAD21	chr4:7429947-7430350	H1-hESC	embryonic stem cell:	n/a	chr4:7430030-7430039
48	RAD21	chr4:7430086-7430343	H1-hESC	embryonic stem cell:	n/a	n/a
49	RCOR1	chr4:7432128-7432458	Hela-S3	cervix:	n/a	n/a
50	RCOR1	chr4:7433448-7433692	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7437027-7437077	LNCaP	prostate:	n/a
2	chr4:7436701-7436751	K562	blood:	n/a
3	chr4:7437027-7437077	LNCaP	prostate:	n/a
4	chr4:7436701-7436751	K562	blood:	n/a
5	chr4:7435639-7435689	GM12878	blood:	n/a
6	chr4:7436861-7436911	HL-60	blood:	n/a
7	chr4:7430936-7430986	HAEpiC	amniotic membrane:	n/a
8	chr4:7436701-7436751	H1-hESC	embryonic stem cell:	embryo
9	chr4:7437156-7437206	AG09309	skin:	n/a
10	chr4:7437156-7437206	HCF	heart:	n/a
11	chr4:7437027-7437077	BE2_C	brain:	n/a
12	chr4:7436701-7436751	HRPEpiC	eye:	n/a
13	chr4:7436259-7436309	HMEC	breast:	n/a
14	chr4:7435357-7435407	CMK	blood:	n/a
15	chr4:7436874-7436924	Caco-2	colon:	n/a
16	chr4:7436693-7436743	GM12878	blood:	n/a
17	chr4:7436239-7436289	AG10803	skin:	n/a
18	chr4:7435357-7435407	IMR90	lung:	fetal
19	chr4:7437027-7437077	NH-A	brain:	n/a
20	chr4:7436259-7436309	GM12891	blood:	n/a
21	chr4:7430936-7430986	CMK	blood:	n/a
22	chr4:7435463-7435513	HCPEpiC	choroid plexus:	n/a
23	chr4:7436701-7436751	RPTEC	kidney:	n/a
24	chr4:7437027-7437077	NHBE	bronchial:	n/a
25	chr4:7436861-7436911	AG04449	skin:	fetal
26	chr4:7435357-7435407	NB4	blood:	n/a
27	chr4:7436701-7436751	CMK	blood:	n/a
28	chr4:7437027-7437077	T-47D	breast:	n/a
29	chr4:7434754-7434804	SK-N-MC	brain:	n/a
30	chr4:7435639-7435689	SK-N-SH	brain:	n/a
31	chr4:7436239-7436289	HRE	kidney:	n/a
32	chr4:7436199-7436249	H1-hESC	embryonic stem cell:	embryo
33	chr4:7435639-7435689	ProgFib	skin:	n/a
34	chr4:7436239-7436289	Caco-2	colon:	n/a
35	chr4:7435639-7435689	Hela-S3	cervix:	n/a
36	chr4:7435639-7435689	HCPEpiC	choroid plexus:	n/a
37	chr4:7434754-7434804	HIPEpiC	eye:	n/a
38	chr4:7430936-7430986	GM12891	blood:	n/a
39	chr4:7434754-7434804	GM19239	blood:	n/a
40	chr4:7430936-7430986	Hela-S3	cervix:	n/a
41	chr4:7436874-7436924	BJ	skin:	n/a
42	chr4:7435463-7435513	AoSMC	blood vessel:	n/a
43	chr4:7436701-7436751	HepG2	liver:	n/a
44	chr4:7435357-7435407	GM12891	blood:	n/a
45	chr4:7434754-7434804	AG09309	skin:	n/a
46	chr4:7436701-7436751	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:7435639-7435689	LNCaP	prostate:	n/a
48	chr4:7437027-7437077	GM12891	blood:	n/a
49	chr4:7436701-7436751	GM19239	blood:	n/a
50	chr4:7435357-7435407	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:7432269..7435967-chr4:7438458..7442398,4	MCF-7	breast:
2	chr4:7426666..7428188-chr4:7440042..7442576,2	MCF-7	breast:
3	chr4:7430206..7433720-chr4:7434978..7437884,3	K562	blood:
4	chr4:7428532..7430154-chr4:7431457..7433548,3	K562	blood:
5	chr4:7428532..7430154-chr4:7431457..7433548,3	K562	blood:
6	chr4:7430997..7432542-chr4:7435254..7438169,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSAPL1-1	chr4:7432021-7433304	NONHSAT095056

Variant related genes	Relation type
PSAPL1	TF binding region
PSAPL1	CpG island
ENSG00000178597	chromatin interactions

Extended variants
information (count: 638 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:638 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4025904	chr4:7427899-7427900	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs547747267	chr4:7427903-7427904	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs139500428	chr4:7427919-7427920	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538263918	chr4:7427920-7427921	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs566470954	chr4:7427933-7427934	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189539033	chr4:7427938-7427939	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs111788128	chr4:7427939-7427940	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549146025	chr4:7427943-7427944	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182174174	chr4:7427997-7427998	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538069666	chr4:7428014-7428015	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs140553436	chr4:7428018-7428019	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35764094	chr4:7428025-7428026	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs11732486	chr4:7428034-7428035	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577733233	chr4:7428045-7428046	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538926054	chr4:7428104-7428105	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372794105	chr4:7428116-7428117	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73086323	chr4:7428117-7428118	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572445354	chr4:7428208-7428209	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs572090997	chr4:7428209-7428210	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs145530834	chr4:7428210-7428211	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs148821397	chr4:7428265-7428266	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs13125782	chr4:7428266-7428267	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs545907466	chr4:7428267-7428268	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs543477224	chr4:7428287-7428288	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs565160603	chr4:7428310-7428311	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs532552334	chr4:7428320-7428321	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs543187502	chr4:7428334-7428335	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs10023533	chr4:7428355-7428356	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs142512509	chr4:7428361-7428362	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs532397954	chr4:7428369-7428370	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs545114862	chr4:7428370-7428371	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs560536515	chr4:7428376-7428377	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs10031234	chr4:7428388-7428389	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs62277595	chr4:7428391-7428392	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs192428550	chr4:7428392-7428393	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs181910452	chr4:7428393-7428394	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs73086327	chr4:7428419-7428420	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs189722670	chr4:7428436-7428437	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs376905333	chr4:7428460-7428461	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs571431170	chr4:7428498-7428499	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs182068683	chr4:7428502-7428503	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs538448318	chr4:7428516-7428517	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs188419841	chr4:7428538-7428539	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs565818248	chr4:7428544-7428545	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs536281181	chr4:7428569-7428570	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs147630844	chr4:7428574-7428575	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs11947343	chr4:7428605-7428606	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs75953090	chr4:7428612-7428613	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs142290769	chr4:7428627-7428628	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs11947344	chr4:7428628-7428629	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:161 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7418800-7429200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:7423200-7436200	Weak transcription	Right Atrium	heart
3	chr4:7425000-7430400	Enhancers	Fetal Muscle Leg	muscle
4	chr4:7425200-7430400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
5	chr4:7425600-7429800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr4:7425800-7429200	Weak transcription	Brain Germinal Matrix	brain
7	chr4:7426200-7428400	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr4:7426600-7429800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:7426600-7431600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr4:7426600-7431800	Weak transcription	Esophagus	oesophagus
11	chr4:7427000-7438800	Weak transcription	Spleen	Spleen
12	chr4:7427200-7428200	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr4:7427200-7431400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr4:7427200-7431400	Weak transcription	HMEC	breast
15	chr4:7427400-7428600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:7427400-7431400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr4:7427600-7429200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr4:7427800-7428800	Weak transcription	Fetal Thymus	thymus
19	chr4:7428200-7433000	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr4:7428400-7428600	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr4:7428400-7432400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr4:7428600-7428800	Enhancers	Right Ventricle	heart
23	chr4:7428600-7429000	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr4:7428600-7429400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr4:7428600-7429400	Bivalent Enhancer	Fetal Stomach	stomach
26	chr4:7428600-7433000	Enhancers	H1 Cell Line	embryonic stem cell
27	chr4:7428600-7433000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr4:7428600-7433800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr4:7428800-7429200	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr4:7428800-7431000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:7429000-7429200	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr4:7429000-7429200	Enhancers	Fetal Thymus	thymus
33	chr4:7429000-7429400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr4:7429000-7431000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr4:7429000-7431600	Weak transcription	Right Ventricle	heart
36	chr4:7429200-7429400	Enhancers	Brain Germinal Matrix	brain
37	chr4:7429200-7429600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr4:7429200-7430000	Enhancers	H9 Cell Line	embryonic stem cell
39	chr4:7429200-7430200	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr4:7429200-7430400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr4:7429200-7430600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr4:7429200-7430800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr4:7429200-7431400	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr4:7429400-7429600	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr4:7429400-7432600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr4:7429600-7430600	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr4:7429600-7432000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr4:7429800-7432000	Enhancers	Fetal Heart	heart
49	chr4:7429800-7432200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr4:7429800-7432600	Enhancers	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links